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31555-59-6

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31555-59-6 Usage

General Description

5-Methyl-thiophene-2-carbonyl chloride is a chemical compound that is derived from the thieno[2,3-b]thiophene structure. It is a carbonyl chloride derivative and is commonly used in organic synthesis and pharmaceutical research. It is a reactive and versatile compound that can be used as a building block for the production of various pharmaceuticals, agrochemicals, and materials. The presence of the carbonyl chloride group makes it an important intermediate for the synthesis of a wide range of compounds, particularly in the production of heterocyclic compounds. It is important to handle this compound with caution, as it may be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 31555-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31555-59:
(7*3)+(6*1)+(5*5)+(4*5)+(3*5)+(2*5)+(1*9)=106
106 % 10 = 6
So 31555-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClOS/c1-4-2-3-5(9-4)6(7)8/h2-3H,1H3

31555-59-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H36784)  5-Methylthiophene-2-carbonyl chloride, 98%   

  • 31555-59-6

  • 250mg

  • 1394.0CNY

  • Detail
  • Alfa Aesar

  • (H36784)  5-Methylthiophene-2-carbonyl chloride, 98%   

  • 31555-59-6

  • 1g

  • 3402.0CNY

  • Detail

31555-59-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methylthiophene-2-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 5-methylthiophen-2-ylcarbonyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31555-59-6 SDS

31555-59-6Relevant articles and documents

Fine-Tuned Photoactive and Interconnection Layers for Achieving over 13% Efficiency in a Fullerene-Free Tandem Organic Solar Cell

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, p. 7302 - 7309 (2017)

Fabricating organic solar cells (OSCs) with a tandem structure has been considered an effective method to overcome the limited light absorption spectra of organic photovoltaic materials. Currently, the most efficient tandem OSCs are fabricated by adopting

Palladium-Catalyzed Electrochemical C-H Bromination Using NH4Br as the Brominating Reagent

Yang, Qi-Liang,Wang, Xiang-Yang,Wang, Tong-Lin,Yang, Xiang,Liu, Dong,Tong, Xiaofeng,Wu, Xin-Yan,Mei, Tian-Sheng

supporting information, p. 2645 - 2649 (2019/04/17)

The palladium-catalyzed electrochemical C-H bromination of benzamide derivatives under divided cells is developed, in which NH4Br serves as a brominating reagent and electrolyte. The protocol avoids the use of chemical oxidants and provides an alternative method for the synthesis of aryl bromides.

7-AZAINDOLE OR 4,7-DIAZAINDOLE DERIVATIVES AS IKK EPSILON AND TBK1 INHIBITOR AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

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Paragraph 0842; 0843, (2016/10/31)

Provided are 7-azaindole or 4,7-diazaindole derivatives as an IKKε (I-kappa-B kinase epsilon) and TBK1 (TANK-binding kinase 1) inhibitor. The 7-azaindole or 4,7-diazaindole derivative effectively inhibits IKKε and TBK1, and thus is useful not only as an a

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